Baxter Medical AB jobb

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. Do you want to make an impact at Baxter's thriving Luleå site in Sweden? We are dedicated to manufacturing Liko patient lifts, slings, and accessories that improve the mobility and care of individuals worldwide. Join our award-winning team, honored with the prestigious Swedish Lean Prize 2021, and contribute to a brighter future at Baxter's Luleå site as Continuous Improvement Engineer! The main purpose of the position is to lead and implement improvement modifications and support the development of continuous improvement, activities towards MIP(cost savings) and Lean Manufacturing on the site. Essential duties and responsibilities: – Other duties may be assigned: Organize, lead and participate in continuous improvement activities to meet set targets. Create project plans and drive projects for continuous improvement, as well as support managers and other teams on this field. Coordinate tasks with internal and/or external service providers. Ensure progress of strategic focus towards world class supply chain by tracking supply chain changes, risks, performance, compliance, and corporate and local plant initiatives. Overall ownership of tracking and follow-up MIP for the site in collaboration with global lead for MIP’s. Coordinate training (for example Green Belt and Lean methods) and coach the business. Lead, develop and standardize analyses and projects for the site. Back-up for the roles within the CI team. Education, experience and qualifications: Education: Bachelor’s degree in Business, Finance, Engineering or Supply Chain. Experience: 5+ years of manufacturing operations experience, 5+ years of knowledge and experience in Lean Manufacturing and Kaizen principles (Experience In a Medical Devices or Life Sciences industry is a plus. Knowledge of Lean tools, Continuous improvement, project management, MS Office. Must be fluent in Swedish and English. Effective written and oral communication skills Competencies: Ability to drive and understand continuous improvement and see the whole process with a focus on customers. Action oriented/drive for results. Ability to prioritize in a fast-paced, changing environment. Analytical approach, eager to cooperate in a team. Effective time management, problem solving and decision-making skills. Proven multi-functional team leader/member.

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. Liko AB är en del av Baxter koncernen och i Alvik utanför Luleå har vi omkring 110 anställda där vi producerar våra patientlyftar, lyftselar och tillhörande produkter. Vi söker nu en operatör till vår Textilproduktionen. På Baxter är vi sammanbundna av vårt uppdrag. Oavsett din roll på Baxter har ditt arbete en positiv inverkan på människor runt om i världen. Du kommer att känna av vårt syfte i hela organisationen, eftersom vi vet att vårt arbete förbättrar resultaten för miljontals patienter. Baxters produkter och behandlingar finns på nästan alla sjukhus världen över, på kliniker och i hemmet. I 90 år har vi varit banbrytande för betydande medicinska innovationer som förändrar vården. På Baxter räddar vi och upprätthåller liv. På vår produktionssite i Alvik, Luleå tillverkar vi Liko personlyftar, selar och lyfttillbehör som används för att förflytta rörelsehindrade personer vid äldreboenden, sjukhus och hem över hela världen. Tillsammans skapar vi en plats där vi är glada, framgångsrika och inspirerar varandra. Det är här du kan göra ditt bästa arbete. Om tjänsten Vi söker nu en operatör till selproduktionen till vår verksamhet i Luleå. Dina huvudsakliga arbetsuppgifter kommer vara att producera våra lyftselar. Vår produktion består av att sy lyftselarna på ett flertal olika symaskiner samt att säkerställa kvalitén på produkten. Vi vann svenska Lean-priset 2021 så vårt Lean-arbete och ständiga förbättringar är en naturlig del av vår verksamhet där du kommer ha en viktig roll. I vår produktion i Alvik utanför Luleå erbjuder vi en ren och modern arbetsmiljö med ergonomiskt anpassade arbetsstationer. Du kommer att ingå i en trivsam arbetsgrupp bestående av 17 medarbetade i mixade åldrar. Vi erbjuder lunch till ett förmånligt pris på vår närliggande restaurang och vi har ett personalgym samt friskvårdsbidrag. Din profil Vi söker dig som är ansvarstagande, pålitlig och öppen för förändringar. För att lyckas i ditt arbete bör du vara en duktig lagspelare som också kan arbeta självständigt. Erfarenhet av sömnad eller att arbeta i en produktion är meriterande men inget krav. Goda kunskaper i svenska språket är ett krav. Andra egenskaper vi värdesätter är att du är noggrann, strukturerad och har en god samarbetsförmåga. Ett krav är att du ska ha fyllt 18 år. Anställningsform Tillsvidare som inleds med 6 månader tidsbegränsad anställning. Det är fördelaktigt att ha körkort och egen bil för att kunna ta sig ut till Alvik då bussförbindelserna är begränsade. Heltid, arbetstid är dagtid kl 7-16. Ansökan Urval och intervjuer sker löpande så tillsättning av tjänsten kan ske innan sista ansökningsdag, så sök nu!

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. Baxter is seeking a Field Service Engineer to join our Technical Services Team in Sweden. The Field Engineer is responsible for the service activity on products supplied by Baxter/Hillrom in the defined geographical areas (preferred regions Göteborg or Stockholm). They will need to undertake their duties in compliance with assigned company procedures (e.g. Control of Service Documentation, Environmental Health & Safety). Key Responsibilities: Install, service, repair and maintain products, distributed by Baxter/Hillrom in the defined area of responsibility as per the defined service documentation and the quality system framework. Establish & maintain timely customer communications & relationships, along with other key stakeholders (e.g. team members and business units). Report all relevant service activity, ensuring updated and accurate service data in the service system (all work orders should be closed within the same day). Responsible for maintaining and documenting the assigned calibration equipment. Provide technical support for in-bound calls from customer & patients, document the job on the system and undertake the relevant actions. Maintain up-to-date technical competence in assigned products by successfully completing the relevant training and development. Identify opportunities for new business or business growth for products & services and escalate to the relevant stakeholders (e.g. account managers, Inside Sales). Review KPIs regularly and adapt the working practices to ensure service level is maximised. Plan and perform qualified technical training to distributors, partners, and colleagues. Co-ordinate and disseminate technical updates and bulletins. Be the technical expert and support for customers, account managers and engineers. This includes being the technical escalation point for the designated product group. Escalate and communicate updates to the monthly SME calls. Represent UKIN interests in EMEA/Global technical community. Provide technical input into contracts & tender submissions. Job Requirements: Degree, HNC/HND or equivalent level qualification in the relevant engineering field In-depth level of practical experience (minimum of 5 years of proven experience) Good IT knowledge on general connectivity, network integration of devices, wireless protocols, mobile network technologies, software support and cyber security standards would be advantageous. Frequent and regular travel within the assigned geographical region in Sweden/Nordic’s. Driving licence Fluid in Swedish and English language Your next step: If you like the sound of the above role, can thrive in a fast-paced working environment and are excited about working in a learning and growth culture, then we’d love to talk to you. Please apply directly on our Online System.

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. We are looking for a Medical Science Liaison (MSL) located in Stockholm, Sweden or Copenhagen, Denmark to join our team. The ideal candidate will have outstanding knowledge in the products and therapeutic areas within a specific segment of Baxter. This field-based position involves assessing and responding to clinical, scientific, or medical inquiries, including discussions initiated by healthcare professionals (HCPs), even if they involve off-label topics. You will play a crucial role in communicating and collaborating with Key Opinion Leaders (KOLs), always prioritizing the patient, and adhering to the highest ethical standards. You will support the Medical Manager/Director in developing and implementing the Medical Affairs vision, mission, strategy, and action plan, ensuring alignment with the business plan for the Nordic region and the Connectivity Solution portfolio at the Western Europe (WEU) level. As a key partner to various country/region functions such as Marketing, Sales, Regulatory Affairs, Patient Access, Compliance, and Legal, the MSL will provide medical-scientific and strategic feedback to country teams. They will also contribute to Connectivity Solutions projects at the WEU level. Effective communication is crucial, and the MSL must adapt their communication style to various teams and individuals. Additionally, they will provide input on interpreting and applying policies and regulations to ensure patient safety and compliance, particularly for low-risk projects. If you are passionate about making a difference in patient care, possess scientific expertise, and thrive in a collaborative environment, we encourage you to apply for this exciting opportunity! Essential Duties and Responsibilities Identify and call out clinical needs from Nordics countries for HST and from WEU for connectivity solutions. Be the primary contact for investigator-initiated trials. Evaluate the effectiveness of connectivity solutions on the patients care workflows and their impact on Caregivers / users. Monitor the scientific literature on the HST therapeutic area/products. Maintain ongoing focus on driven and industry trends in the medical/scientific dissemination of information. Assist in the development of publication plans. Support the Medical Manager/Director in the review of promotional materials, Act as a liaison with the medical community (medical professional societies, therapeutic area experts/KOLs, investigators, consultants). Support the Medical Manager/Director in the collaboration with KOLs and the development of KOL programs. Apply engagement channels to gain medical/scientific insights and serve as a credible resource within Baxter as well as customers. Assist in development of medical-scientific advisory boards, symposia, and publication planning. Provide accurate and fair balanced medical-scientific education and information on products, therapies, issues, trends, clinical research, etc. during external training. Educate and trains internal staff on therapies, issues, trends, clinical research, etc. as well as provide scientific support to sales teams and present technical or complex information in a clear, concise, organized manner. Support the Medical Manager/Director in the risk management of field products and the resolution of field issues related to the clinical use of products. Ensure compliance of promotional materials. The role will involve covering the Nordics region 50% and western Europe for connectivity 50%. Travel across Europe will be essential. Qualifications A mature personality with excellent interpersonal skills and the ability to interact with multiple partners (internal and external) and to build relationships of credibility and trust with them. Excellent product knowledge and expertise. Excellent presentation, medical writing and oral communications skills in Swedish/Danish and English. Proven teaching capabilities and understanding of adult learning concepts. Strong analytical and problem-solving skills. Ability to search and summarize medical literature/data accurately and appropriately. Able to work as part of a team & participate cross-functionally. Broad understanding of the regulatory and healthcare environment in the Nordics region. Education and/or Experience Excellent scientific and medical background to disseminate and discuss scientific evidence and complex medical information: Bachelor’s degree in chemistry, biology, pharmacy, or other medical/nursing/paramedic related field with proven MSL or medical affairs manager experience (2 years). Experience in MS Office applications. Experience with literature review (analysis and synthesis). Experience in public presentation. Clinical trial experience with solid understanding of GCP and training in reporting of adverse events is a plus. What we can offer Being part of a digital journey and exiting product innovations. Great team and work atmosphere. A company focusing on Inclusion and Diversity. If you like the sound of the role and if this role resonates with you, then we’d love to talk to you!

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. Summary Now we are looking for a Senior Product Quality Engineer in Alvik, Luleå. This is where you are the quality R&D representative for all design & development areas of our Medical Device products,being a part of our important mission to save and sustain lives. You will partner with the R&D Engineering team in the design maintenance of EU-MDR 2017/745 and FDA patient lifting systems on safe patient handling medical devices to ensure that design control principles are followed, and that safety and efficacy are demonstrated. At all times throughout the process, you will identify and mitigate risks. Essential Duties and Responsibilities: Provide Product Quality (R&D Quality) assurance support and oversight for in the Patient Support Systems division for medical devices in care environments on patient lifting systems on safe patient handling. Supporting all Product Quality priorities in multifunctional and international teams for the site Lulea (Sweden) on all Quality and R&D programs. Further support of the Pluvigner (France) and other sites as needed. Provide quality assurance support and oversight for product design activities including: Design and Development Planning, Design Input, Design Output, Design Review, Design Verification and Validation, Design Transfer, Design Changes. Ensure compilation and maintenance of product Design History Files in collaboration with R&D. Partner with Sustaining Engineering and Research & Development to ensure design reviews are thorough and robust. Review and approve Design Verification and Validation test plans, protocols and reports; guide the use of robust statistical techniques. Document traceability of requirements through design output and to design verification and/or design validation. Insist on early requirements maturation, early test plan/script development, and design input requirements that are indicative of real-world use case environment and customer needs. Review intended use validation for non-product software and tools used in the development process. Actively participate with design teams on developing product Risk Management Files; ensure risk assessments adequately address safety and efficacy and are compliant to the highest standards. Perform DHF audits of other products as an independent reviewer. Support external regulatory and customer audits. Collaborate with the global Product Quality team to drive continuous improvement, including development of standard work, striving for a world-class Product Development Process. Ensure R&D Quality aspects of complaints, CAPAs, Field Actions etc. are being handled with highest priority to ensure patient safety, highest quality and compliance. Audit Support for internal, corporate, and external audits regarding as needed. Establishment of applied standards as design input for products in collaboration with R&D and assuring conformance to regulations in the area of responsibility. Qualifications Bachelor’s degree in Engineering or Computer Science or similar field. 5+ years’ experience in Quality, Software Engineering or related field. Experience in assessing and developing acc. to procedure to meet Medical Device and Software Connectivity regulatory requirements and guidance’s. Experience with ISO/ Notified Body audits. FDA inspections is a plus. Experience in the application of design controls and compliance requirements in accordance with ISO 13485, ISO 14971, EU-MDR 2017/745, IEC 62304, 21 CFR Part 820, 803, & 806, 21st Century Cures Act, NIST Cybersecurity framework, FDA pre and post market cybersecurity guidance. Professional certification such as ASQ, IEEE, Six Sigma, LEAN manufacturing or achievement of certification. ASQ CSQE preferred. Strong communication and leadership skills. Strong, results driven, project management skills. Excellent problem-solving skills and the ability to teach others. Capable of clearly presenting and justifying quality position and requirements to management. Make an impact at Baxter's thriving Luleå site in Sweden. We are dedicated to manufacturing Liko patient lifts, slings, and accessories that enhance the mobility and care of individuals worldwide. Join our award-winning team, honored with the prestigious Swedish Lean Prize 2021, and contribute to a brighter future at Baxter's Luleå site.

JOB SUMMARY: Now we are looking for an Accounting Manager in Kista, Stockholm. The role of the NORDICS Accounting Manager is to ensure accuracy and integrity of US GAAP and statutory financial reporting within the Nordics region, provide expertise in complex accounting matters and decisions, and build strong partnership with Shared Service Centre, local country finance, commercial and other functional organizations to support financial and accounting processes in compliance with US GAAP and statutory requirements and company’s policies and procedures. ESSENTIAL DUTIES AND RESPONSIBILITIES: – Other duties may be assigned: You will be responsible for ensuring accuracy and integrity of US GAAP and statutory financial reporting for the countries in scope and provide expertise in complex accounting matters and decisions. You will be responsible for statutory tax compliance for the countries in scope and completing tax filings. You will be also responsible for ensuring all external legal and statutory reporting and filing obligations are met on behalf of the Directors. Examples such as Intrastat, VAT, Government mandated statistics, Income tax and other. You will provide local support to country management. You will maintain strong relationship with key partners: local business, operations and decision support management. Provide Country sales and service management support as necessary. You will be responsible for ensuring the completion of all accounting transactions (Accruals, prepaid, Revenue deferments) in an efficient, cost-effective manner, and supports Account Receivable and Accounts Payables when necessary. You will ensure that the timely completion of all period closing requirements and the consistent application of all accounting & company policies You will prepare country level balance sheet and cash flow reviews You will ensure the timely completion of all local statutory reporting, audit, and tax requirements You will provide JDE expertise; coordination of training to fulfill local needs You will coordinate of local efforts to achieve Sarbanes-Oxley compliance (SOX), including any required testing, training and process or control improvements required You will be the contact person for authorities or other external parties, such as auditors, banks, etc. EDUCATION, EXPERIENCE AND QUALIFICATIONS: University graduate in finance/accounting At least 5 years of experience in accounting and finance; Must be familiar with U.S. GAAP Proven experience in a multinational environment and/or audit. International experience required; Experience with U.S. company strongly preferred Full or partial accounting qualification such as ACCA or CIMA is required Fluent in English and Swedish Inquisitive nature Detailed knowledge of local GAAPs for the countries in scope Strong process and continuous improvement skills Supportive, positive attitude and approach to work Able to work independently or as part of a team Good PC and software skills; Microsoft products a must; JD Edwards or similar ERP system strongly preferred What we can offer An exciting opportunity for you and a chance to work in a diverse and experienced team with a great mix of people. Joining Baxter means joining a team that you can truly learn from! Independent position with an opportunity to build your own strategy and make a real impact. A chance to further build your professional experience in the area of health care. Internal training tailored to business needs and career goals. Stability of employment in a recognizable and established company.

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. As a Quality Manager you ensure product quality through the implementation of various control and improvement opportunities and coordination of work within the area of Quality Management system, CAPA and Learning Management system. Support to Sr. QA Manager in ensuring that processes needed for the quality management system are established, implemented, and maintained. Ensure the promotion of awareness of regulatory and customer requirements throughout the organization. Essential Duties and Responsibilities Management and further development of the QMS Team Intelligently deploy resources to meet daily business needs in a timely manner while evolving the work processes to become more proactive, efficient, and effective Provide strategic direction and leadership to the team to ensure operations adhere to requirements of compliance and product quality Define and coordinate tasks within the scope of the objective and task definition, as well as review and discuss work results Plan and execute local Audit program Control and track the products and processes quality and regulatory compliance through adequate performance metrics and plans. Stop, if required, the delivery and/or the production of products in case of non-conformity. Ensure that adequate records of data and results concerning tests and product controls are taken Manages effective cross-function relationships and in particular work with concept, product and commercialization teams to ensure quality of product and process. Drive data analysis of performance data to identify high priority issues relating to safety, regulatory compliance and customer satisfaction. Coordination of resources within area of Quality Management system, CAPA and Learning Management system Continuous improvements of processes within area of responsibility Implementation of the company-specific quality policy and quality goals Ensuring product conformity, reducing production deviations Ensuring compliance with design and development activities Communication of the quality principles to promote quality awareness in the company Ensuring compliance with production and process controls Ensuring product conformity, reducing production deviations Ensuring compliance with acceptance and validation activities Management of non-compliant products and investigation of problems with regards to product quality, as well as support for processing: Carry out root cause analyzes, introduce corrective measures to eliminate or reduce the identified causes. Serve as primary point of contact for quality and regulatory issues related to manufacturing processes Lead efforts to identify and execute initiatives to improve manufacturing process and product quality EDUCATION, EXPERIENCE AND QUALIFICATIONS: Proficient with Quality System Regulations, IS013485, Medical Device Regulation and ISO 13485 Quality System Standards. Demonstrated ability to succeed in team environments and possesses effective interpersonal skills. Demonstrated attention to detail, analytical decision-making, and problem-solving skills. Proven ability to succeed in an environment of continuous improvement and to identify improvement opportunities. Strong customer orientation and excellent written and verbal communication skills. Ability to effectively navigate rapidly changing quality, regulatory and business environments and succeed in an environment of change. Bachelor’s degree (minimum) in an Engineering field, preferable mechanical, electrical, or industrial engineering. 5+ years of experience in Quality Assurance or Regulatory Affairs in the Medical Device or Pharmaceutical industry. Strong management and analytical skills Strong process and continuous improvement skills Supportive, positive attitude and approach to work Good communication skills, both verbal and written Able to work independently or as part of a team Strategic skills, ability to holistic/global perspective Additional training in Risk Management, Six Sigma, Lean Manufacturing and Statistical Methods is preferred. Experience of an R&D and production site is a plus Fluent in Swedish and English, other languages are beneficial

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. We are now looking for an Account Manager in mid / south of Sweden to continue to drive the growth of our Infusion Therapies & Technologies portfolio. In this role you will focus on Clinical Nutrition and Fluid management targeting healthcare professionals within the hospital setting. You will join a growing Business Unit in the spotlight and continue to expand Baxter’s Infusion Therapies & Technologies business. Our Nordic team consists of highly professional and passionate colleges where we strive to collaborate and support each other to find the best possible solution. You have strong social and communication skills, both when writing and speaking. You enjoy being in front of a crowd presenting and thrive when you are negotiating with prospects. You are quick to understand and adapt – especially when our customers’ needs change. Essential Duties and Responsibilities Develop and manage relationship with customers, expand existing accounts and build new relationships within your territory. Achieving sales targets and implementing sales strategies to attain sales volume, customer growth and customer satisfaction for the portfolio. Participate in developing strategic plans for the products and related services in Sweden. Preparation and implementation of targeted account plans; you will propose and provide each customer with appropriate solutions that will increase opportunities both for the customer and for Baxter. Actively drive development and implementation of targeted tender plans, including pre-tender strategies and tactics. Qualifications Medical background with hospital experience, preferably nurse or dietitian by education. A genuine drive and curiosity for sales with an understanding of strategic account development with strong eye for business. Selling, educating and informing is natural to you and you are good at creating and developing long-term relationships. Both remote and face-to-face. Strong negotiation skills with good knowledge about the health care system and the relevant customers involved in the selling and tender processes. Adaptable, proven communication, teamwork and team building skills. A can-do attitude, outspoken and with a positive energy is the personality we are looking for Driver’s license is required. Proficiency in Swedish as well as strong English language is great. What we can offer A developing opportunity for you and a chance to work in a diverse and experienced team with a phenomenal mix of people. Joining Baxter means joining a team that you can truly learn from! Independent position with an opportunity to build your own strategy and make a real impact. A chance to further develop your professional experience in health care. Internal training tailored to business needs and career goals. Field based job You will gain excellent exposure and fantastic industry knowledge within the territory working for a global organization. If you like the sound of the above role and if this role resonates with you, then we’d love to talk to you!